Methadose Dispersible Tablet
Product Images NDC 0406-0540

3 FDA label images from Specgx Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Methadose Dispersible (NDC 0406-0540). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Specgx Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Chemical Structure (Methadose Dispersible Tablets 1)

Chemical Structure (Methadose Dispersible Tablets 1)
Chemical structure diagram of Methadone Hydrochloride showing the molecular formula C21H27NO with HCl and molecular weight of 345.91.*
FDA Label Image

Methadose 40mg (Methadose Dispersible Tablets 2)

Methadose 40mg (Methadose Dispersible Tablets 2)
METHADOSE 40 mg dispersible tablets label for oral suspension. The label states Methadone Hydrochloride USP 40 mg per tablet, with 100 tablets in the container. It includes storage instructions, dosage guidance to see accompanying literature, and warnings about seal integrity. Manufactured or labeled by SpecGx LLC, Webster Groves, MO, and branded as Mallinckrodt.*
FDA Label Image

Methadone 40mg (Methadose Dispersible Tablets 3)

Methadone 40mg (Methadose Dispersible Tablets 3)
Label for Methadone Hydrochloride Tablets, 40 mg, oral dispersible tablets with orange flavor, marketed by SpecGx LLC. The label includes NDC 0406-2540-01, indicates 100 tablets per package, and states the product is Rx only. Usage instructions and storage conditions are partially visible, with a caution to keep tightly closed and store between 20° to 25°C.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.